217.895 Inspections -- Records of pharmacy.

208 words·~1 min read·/ky/chapter-217/217-895

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

(1)Routine inspections of pharmacies for compliance with KRS 217.815 to 217.826

shall be undertaken by the Kentucky Board of Pharmacy.

(2)Every pharmacy shall retain for a period of two

(2)years from July 15, 1982, a

pharmacy record of all prescribed drug and biological products dispensed. The

pharmacy record shall be retained for the purpose of providing valid data for bona

fide research and reporting to the General Assembly as to the effectiveness of KRS

217.815 to 217.826. The pharmacy record shall include:

(a)The brand name of the drug or biological product, when applicable.

(b)The name of the manufacturer or the supplier of the drug or biological

product, if the drug or biological product has no brand name.

(c)The strength of the drug or biological product, when significant.

(d)The quantity dispensed, when applicable.

(e)The serial number of the prescription.

(f)The date the prescription was originally dispensed and refilled.

(g)The name of prescribing practitioner.

(h)The name of patient for whom the drug or biological product was prescribed.

(i)The price for which the drug or biological product was sold to the purchaser.

(j)A notation if the practitioner indicated "Do not substitute" or the purchaser

refused the product selected.